Product Details

SNP ID: rs139944275
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.18:57352987 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCACCACTCCCAAGTACGCCAGCCC[C/G]GGGGCGCCCCGAATGTACATGTTCC
Phenotype: MIM: 609478
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: ST8SIA3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015879.2	498	Silent Mutation	CCC,CCG	P47P	NP_056963.2